Notice Type
Departmental
Consent to the Distribution of Changed Medicines Pursuant to section 20 of the Medicines Act 1981, the Minister of Health hereby consents to the distribution in New Zealand of the changed medicines which were referred to the Minister of Health under the provisions of section 24 (5) of the Act and are set out in the Schedule hereto: Schedule Name and Strength Form Name and Address of Manufacturer Proprietary Name(if any) Orciprenaline sulphate 0.75 mg per dose Spray, oral, metered dose Boehringer Ingelheim KG., Ingelheim am Rhein, Germany Alupent Inhaler Ciprofloxacin hydrochloride 58.22 mg/mL, 116.44 mg/mL equivalent to 50 mg/mL, 100 mg/mL ciprofloxacin and diluent Microcapsules for suspension Bayer AG., Leverkusen, Germany Ciproxin Suspension Dalteparin sodium 10,000 IU in 1 mL, 4 mL Injection, ampoule Pharmacia & Upjohn, Stockholm, Sweden Fragmin Dalteparin sodium 2,500 IU in 0.2 mL, 25,000 IU/mL in 0.2 mL, 0.4 mL, 0.5 mL, 0.6 mL, 0.72 mL Injection, prefilled syringe Pharmacia & Upjohn, Stockholm, Sweden Fragmin Dalteparin sodium 10,000 IU in 1 mL, 4 mL Injection, ampoule Pharmacia & Upjohn, Stockholm, Sweden Fragmin Dalteparin sodium 2,500 IU in 0.2 mL, 25,000 IU/mL in 0.2 mL, 0.4 mL, 0.5 mL, 0.6 mL, 0.72 mL Injection, prefilled syringe Pharmacia & Upjohn, Stockholm, Sweden Fragmin Lenograstim 13.4 MIU Injection, powder, vial Chugai Pharmaceutical Co Limited, Utsonomiya, Tochigi, Japan Granocyte 13 Lenograstim 33.6 MIU Injection, powder, vial Chugai Pharmaceutical Co Limited, Utsonomiya, Tochigi, Japan Granocyte 34 Human chorionic gonadotrophin 500 IU, 1500 IU, 5000 IU; sodium chloride as diluent Injection, powder for, ampoule; Diluent, ampoule Organon International BV., Oss, The Netherlands Pregnyl Finasteride 1 mg Tablet, film coated Merck Sharp & Dohme Limited, Hoddesdon, Hertfordshire, England; Merck Sharp & Dohme Limited, Cramlington, Northumberland, England and Merck Sharp & Dohme (Australia) Pty Limited, South Granville, New South Wales, Australia Propecia Epoetin beta 1000 IU, 2000 IU, 5000 IU, 10,000 IU equivalent to 8.3 g, 16.6 g, 41.5 g and 83 g epoetin; and water for injections as diluent Injection, powder for, vial; Diluent, ampoule Boehringer Mannheim GmbH., Mannheim, Germany Recormon Vigabatrin 500 mg, 1 g Powder, oral, sachet Marion Merrell Dow France SA., Bourgoin-Jallieu Cedex, France Sabril Dated this 30th day of November 1997. G. R. BOYD, Chief Advisor, Regulation and Safety, pursuant to delegation given by the Minister of Health on 20 February 1997.
Publication Date
4 Dec 1997

Notice Number

1997-go8802

Page Number

4052